# FDA Inspection 1102731 - DynaFlex - September 05, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/dynaflex/0226fb05-c7a0-4f3a-a4db-17fc00be71c8
Source feed: FDA_Inspections

> FDA Inspection 1102731 for DynaFlex on September 05, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1102731
- Company Name: DynaFlex
- Inspection Date: 2019-09-05
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/dynaflex/a805d418-c220-4dcf-8f82-08ee4c075100

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7